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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04574180
Other study ID # TSA-2017-6723
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2017
Est. completion date September 9, 2019

Study information

Verified date February 2023
Source TC Erciyes University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Objective: Early loss of primary teeth due to caries, can cause occlusion disorders, aesthetic problems, nutritional problems, abnormal language habits, speech disorders and psychological problems temporary or permanent. The purpose of this study was to evaluate the success of using prefabricated aesthetic crowns for the restoration of excessive tooth loss. Study design: In this randomized, non-blinded clinical study a total of 45 teeth were included, primary molars and anterior teeth and requiring restoration after root canal treatment. Stainless steel(SCC), zirconia(ZC) and strip(S) crowns compared clinically, radiographically and periodontally during follow up period for 6 months. Parents were asked to fill out questionnaire at the 1st and 6th months to evaluate the satisfaction level. In addition, patients' pain and discomfort level was assessed using the visual analogue scale (VAS) scale.


Description:

The color of crowns made it impossible to blind during clinical assessment. Thus, this study was a non-blinded, randomised, and prospective clinical trial. Sample size: This study included 20 maxillary anterior and 25 posterior teeth that required restoration due to excessive material loss. The study groups were: Zirconia crown(ZC) restoration on the primary central and lateral tooth with root canal treatment (n = 10), strip crown(S) restoration on the primary central and lateral tooth with root canal treatment (n = 10), Zirconia crown(ZC) restoration on primary teeth with root canal treatment (n = 12), Stainless-steel crown(SSC) restoration on primary teeth with root canal treatment (n = 13). Clinical Procedure: Assessment Clinical assesment: Table 1 Gingival scores: Löe and Silness Gingival Index(GI)[Löe, 1967]. Periapical radiographic evaluation: Preoperative and every follow up visit. (Radiographic assesment: Table 2) Intraoral photos (standard method): before treatment, after treatment and at every follow-up visit. Crown restoration: All caries were removed after administration of local anaesthesia and proper isolation. Calcium hydroxide/iodoform paste (Vitapex®) pulpectomy was performed according to the guideline. Teeth were restored with a composite resin Nova Resin (IMICRYL®, Konya, Turkey) and glass ionomer cement (MERON®, Voco, Germany) was used as a base material. Strip Crown Forms (3M-ESPE, St. Paul,Minnesota, USA) were used to restore teeth group SC. ZC group (NuSmile, Houston, Tex. the USA) and SCC(3M ESPE, Minnesota, USA) used. Visual analogue scale(VAS): 0-2: no pain/discomfort 4-6:moderate 8-10: high pain/discomfort. The child was asked to choose his/her feelings about the tooth after the procedure and in follow-up appointments. Parents were asked to complete their satisfaction surveys, including the post-op and 6-month controls for patient satisfaction assessment. Statistical Method: IBM® SPSS® Statistics V23 analysed data. The Mann-Whitney U and Chi-square tests were used for intergroup comparisons within the anterior and posterior regions. The Friedman and Cochrane Q tests were used for intra-group time-wise comparisons. Analysis results were presented as the median (q1-q3) and frequency (percentage). P<0.05 was considered statistically significant. Table 1: Clinical assesment Crown retention 0= yes 1= no Individual modified gingival index 0= healthy 1= mild gingival bleeding with a papillus 2= severe inflammation Plaque index 0= no plaque 1. = presence of plaque as a film in the gingival margin 2. = presence of moderate plaque 3. = plaque covering a large number of surfaces Color change 0 = no coloring 1. = minor coloration 2. = noticeable coloration Buccal strip crown surface 0 = no loss 1 = less than 50% loss 2 = more than 50% loss 4 = loss of the entire surface Surface abrasion of the antagonist teeth 0= no abrasion 1. abrasion started on the incisal surface of the casps 2. abrasion more than on the casps Position of the crowns regarding gingival margin 0= subgingival 1= supragingival Occlusion 0= contact (marked or superficial) 1= no contact Condition of the antagonistic tooth 0= natural tooth 1. restored tooth 2. stainless steel crown 3. aesthetic crowns Location on the arch curve 0= normal alignment 1. with rotation 2. wrong position Proximal contacts 0= good (floss passing) 1= weak, no contact Table 2. Postoperative Radiographic Evaluation Criteria and Scores Radiographic evaluation of crown margins 0=good adaptation, continuity in crown contractions 1. small radiolucent area under the restoration 2. huge openings 3. loss of restoration Radiographic evaluation 0= healthy, no pathology 1. presence of a pathology that does not require immediate treatment 2. presence of pathology requiring immediate treatment Radiographic evaluation of pulpal treatment 0=appropriate root treatment 1. short or overflowed root treatment 2. failed pulpal treatment 3. tooth with no pulpal treatment


Recruitment information / eligibility

Status Completed
Enrollment 22
Est. completion date September 9, 2019
Est. primary completion date March 9, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 3 Years to 11 Years
Eligibility Inclusion Criteria: 1. Patients without systemic disease The American Society of Anesthesiologists (ASA)1-2, 2. Patients under 10 years old to perform endodontic treatment for adequate root support 3. Clinical and radiographically confirmed dental caries scored international caries detection and assessment system(icdas) criteria 4-5. 4. Patient/parent approve Exclusion Criteria: 1. Patients with systemic and mental diseases 2. Acute abscess or mobility 3. Internal or external resorption 4. Inadequate oral hygiene after oral health motivation that contraindicate root canal treatment 5. Need for endocarditis prophylaxis 6. Temporomandibular joint(TMJ) disorders, bruxism 7. Absence of antagonistic teeth

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Dental Crown
Pediatric size dental crown; restore damaged tooth to its normal shape, size, and function.

Locations

Country Name City State
Turkey Erciyes University Kayseri?

Sponsors (1)

Lead Sponsor Collaborator
TC Erciyes University

Country where clinical trial is conducted

Turkey, 

References & Publications (5)

El Makawi Y, Khattab N. In Vitro Comparative Analysis of Fracture Resistance of Lithium Disilicate Endocrown and Prefabricated Zirconium Crown in Pulpotomized Primary Molars. Open Access Maced J Med Sci. 2019 Dec 13;7(23):4094-4100. doi: 10.3889/oamjms.2019.864. eCollection 2019 Dec 15. — View Citation

Lee JH. Guided tooth preparation for a pediatric zirconia crown. J Am Dent Assoc. 2018 Mar;149(3):202-208.e2. doi: 10.1016/j.adaj.2017.08.048. Epub 2018 Feb 1. — View Citation

Seminario AL, Garcia M, Spiekerman C, Rajanbabu P, Donly KJ, Harbert P. Survival of Zirconia Crowns in Primary Maxillary Incisors at 12-, 24- and 36-Month Follow-Up. Pediatr Dent. 2019 Sep 15;41(5):385-390. — View Citation

Sonbol HN, Al-Bitar ZB, Shraideh AZ, Al-Omiri MK. Parental-caregiver perception of child oral-health related quality of life following zirconia crown placement and non-restoration of carious primary anterior teeth. Eur J Paediatr Dent. 2018 Mar;19(1):21-28. doi: 10.23804/ejpd.2018.19.01.04. — View Citation

Walia T, Brigi C, KhirAllah ARMM. Comparative evaluation of surface roughness of posterior primary zirconia crowns. Eur Arch Paediatr Dent. 2019 Feb;20(1):33-40. doi: 10.1007/s40368-018-0382-4. Epub 2018 Oct 20. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Visual examination The incidence of crown retention, gingival index, marginal crown localisation 6 months follow up period
Primary Radiographic evaluation Periapical film: the rate of radiolucency. According to the index, each tooth was categorized as having a normal periapical structure (score 1), small changes in bone structure (score 2), changes in bone structure with some mineral loss (score 3), periodontitis with well-defined radiolucent areas (score 4), or severe apical periodontitis with exacerbating features (score 5) 6 months follow up period
Secondary Questionaire A Visual Analogue Scale (VAS): no pain (0-4 mm), mild pain(5-44 mm), moderate pain (45-74 mm), and severe pain (75-100 mm) 6 months follow up period
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